KR970001357A - Benzimidazole derivatives containing conjugated pyridine - Google Patents

Benzimidazole derivatives containing conjugated pyridine Download PDF

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Publication number
KR970001357A
KR970001357A KR1019950016621A KR19950016621A KR970001357A KR 970001357 A KR970001357 A KR 970001357A KR 1019950016621 A KR1019950016621 A KR 1019950016621A KR 19950016621 A KR19950016621 A KR 19950016621A KR 970001357 A KR970001357 A KR 970001357A
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South Korea
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group
atom
hydrogen atom
structural formula
following structural
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KR1019950016621A
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Korean (ko)
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KR0154281B1 (en
Inventor
염을균
최중권
조성윤
강승규
김성수
박경호
황기준
천혜경
김효정
양성일
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강박광
재단법인 한국화학연구소
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Priority to KR1019950016621A priority Critical patent/KR0154281B1/en
Priority to PCT/KR1996/000091 priority patent/WO1997000875A1/en
Publication of KR970001357A publication Critical patent/KR970001357A/en
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Publication of KR0154281B1 publication Critical patent/KR0154281B1/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • C07D491/044Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • C07D491/052Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being six-membered
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • C07D491/044Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • C07D491/048Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered

Abstract

본 발명은 포유동물의 위상분비 억제능력을 보유하고 있어 항궤양제의 유효성분으로서 매우 유용한 다음 구조식(Ⅰ)로 표시되는 접합고리 피리딘을 함유한 벤즈이미다졸 유도체에 관한 것이다.The present invention relates to a benzimidazole derivative containing a conjugated ring pyridine represented by the following structural formula (I), which has a mammalian phase secretion inhibitory ability and is very useful as an active ingredient of an antiulcer agent.

상기 식에서, R은 수소원자, 할로겐원자, C1∼C3의 알콕시, C1∼C3의 할로알콕시 또는 C1∼C3의 할로알킬기 이고; X는이고; R1, R2 ,R3, R4, R5및 R6은 서로 같거나 다른 것으로서 수소원자, 할로겐원자 또는 C1∼C3의 알킬기를 나타내되 다만, 모두 수소원자인 경우에는 제외한다.Wherein R is a hydrogen atom, a halogen atom, C 1 -C 3 alkoxy, C 1 -C 3 haloalkoxy or C 1 -C 3 haloalkyl group; X is ego; R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are the same as or different from each other and represent a hydrogen atom, a halogen atom or an alkyl group of C 1 to C 3 , except when all are hydrogen atoms.

Description

접합고리 피리딘을 함유한 벤즈이미다졸 유도체Benzimidazole derivatives containing conjugated pyridine

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음As this is a public information case, the full text was not included.

Claims (7)

다음 구조식(Ⅰ)로 표시되는 접합고리 피리딘을 함유한 벤즈이미다졸 유도체.Benzimidazole derivatives containing the conjugated ring pyridine represented by the following structural formula (I). 상기 식에서, R은 수소원자, 할로겐원자, C1∼C3의 알콕시, C1∼C3의 할로알콕시 또는 C1∼C3의 할로알킬기 이고; X는이고; R1, R2, R3, R4, R5및 R6은 서로 같거나 다른 것으로서 수소원자, 할로겐원자 또는 C1∼C3의 알킬기를 나타내되 다만, 모두 수소원자인 경우는 제외한다.Wherein R is a hydrogen atom, a halogen atom, C 1 -C 3 alkoxy, C 1 -C 3 haloalkoxy or C 1 -C 3 haloalkyl group; X is ego; R 1 , R 2 , R 3 , R 4 , R 5 and R 6 , which are the same as or different from each other, represent a hydrogen atom, a halogen atom or an alkyl group of C 1 to C 3 , except that all are hydrogen atoms. 제1항에 있어서, 상기 R이 수소원자, 염소원자, 브롬원자, 플루오르원자, 메톡시기, 에톡시기, 프로필옥시기, 트리플루오로메틸기 또는 2,2-디플루오로에톡시기인 것을 특징으로 하는 접합고리 피리딘을 함유한 벤즈이미다졸 유도체.The method of claim 1, wherein R is a hydrogen atom, chlorine atom, bromine atom, fluorine atom, methoxy group, ethoxy group, propyloxy group, trifluoromethyl group or 2,2-difluoroethoxy group, characterized in that Benzimidazole derivatives containing conjugated pyridine. 제1항에 있어서, 상기 R1, R2, R3, R4, R5및 R6가 각각 같거나 다른 것으로서 수소원자, 메틸기, 에틸기 또는 프로필기(다만, 모두 수소원자인 경우에는 제외) 인것을 특징으로 하는 접합고리 피리딘을 함유한 벤즈이미다졸 유도체.The method according to claim 1, wherein R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are the same or different, respectively, hydrogen atom, methyl group, ethyl group or propyl group (except when all are hydrogen atoms) Benzimidazole derivatives containing conjugated pyridine, characterized in that the. 다음 구조식(Ⅰ)로 표시되는 벤즈아미다졸 유도체 및 이들의 약학적으로 허용가능한 염을 유효성분으로 함유하고 있는 것을 특징으로 하는 위궤양 치료제 조성물.Benzamidazole derivatives represented by the following structural formula (I) and pharmaceutically acceptable salts thereof as an active ingredient, gastric ulcer therapeutic composition characterized in that it contains. 상기 식에서, R과 X는 상기 특허청구위 범의 제1항에서 정의한 바와 같다.Wherein R and X are as defined in claim 1 of the claims. 제4항에 있어서, 상기 약제학적으로 허용가능한 염은 산부가염 또는 나트륨염인 것을 특징으로 하는 위궤양 치료제 조성물.The gastric ulcer therapeutic composition according to claim 4, wherein the pharmaceutically acceptable salt is acid addition salt or sodium salt. 제4항에 있어서, 상기 R1, R2, R3, R4, R5및 R6가 각각 같거나 다른 것으로서 수소원자, 메틸기, 에틸기 또는 프로필기(다만, 모두 수소원자인 경우에는 제외)인 것을 특징으로 하는 의궤양 치료제 조성물.The method according to claim 4, wherein R 1 , R 2 , R 3 , R 4 , R 5, and R 6 are the same or different, and each hydrogen atom, methyl group, ethyl group or propyl group (except when all are hydrogen atoms) An ulcer treatment composition, characterized in that. 다음 구조식(Ⅰ)로 표시되는 화합물 제조에 유용한 다음 구조식(Ⅴ)로 표시되는 화합물.A compound represented by the following structural formula (V) useful for the preparation of a compound represented by the following structural formula (I). 상기 식에서, R과 X는 상기 특허청구의 범위 제1항에서 정의한 바와 같다.Wherein R and X are as defined in claim 1. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019950016621A 1995-06-21 1995-06-21 Benzimidazole derivatives containing fused pyridines KR0154281B1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
KR1019950016621A KR0154281B1 (en) 1995-06-21 1995-06-21 Benzimidazole derivatives containing fused pyridines
PCT/KR1996/000091 WO1997000875A1 (en) 1995-06-21 1996-06-12 Benzimidazole derivatives containing fused pyridine

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1019950016621A KR0154281B1 (en) 1995-06-21 1995-06-21 Benzimidazole derivatives containing fused pyridines

Publications (2)

Publication Number Publication Date
KR970001357A true KR970001357A (en) 1997-01-24
KR0154281B1 KR0154281B1 (en) 1998-11-16

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